EUDAMED workshop Stuttgart

Introduction to the EUDAMED Workshop

The European Commission is organising a free registration hybrid workshop in Stuttgart to support the EUDAMED onboarding of all concerned actors, in view of the mandatory use of Actors, UDI/Devices, Notified bodies and Certificates and Market surveillance modules of the system. The workshop will provide an overview of the obligations under the Medical Devices Regulations (Regulation (EU) 2017/745 – MDR, and Regulation (EU) 2017/746 – IVDR) regarding EUDAMED and practical guidance on its use.

The workshop is a good opportunity for economic operators, notified bodies, national authorities, and other stakeholders to prepare for compliance with the Regulations in the context of EUDAMED.

In addition to this first session in Stuttgart, two other workshops with identical content will be held: on 8 October in Rome, Italy, and on 3 December in Brussels, Belgium. All workshops will also be available via online streaming for approved online participants. Please note that registration (both physical and online) for the workshops in Rome and Brussels will open at a later stage.

For the Stuttgart workshop, in order to ensure balanced geographical representation, physical participation will be prioritised for stakeholders based in Germany, Austria, Hungary, Poland, the Czech Republic, and Slovakia.

Below, you will find more information about the workshop, its objectives, and what participants can expect. For all practical information, such as timing and content, please go to the Practical Information tab.

What is EUDAMED?

EUDAMED is the European Database on Medical Devices. It is a centralised system created to improve transparency, traceability, and information sharing in the medical devices sector. EUDAMED supports the implementation of the MDR and the IVDR. It is designed to:

Provide a unique European platform for registration of information on medical devices.
Enhance patient safety by improving public access to data on medical devices.
Support compliance with EU regulations.

The database is an essential tool for all stakeholders to be compliant with MDR and IVDR, making it essential to understand its functions and requirements.

Workshop Objectives

The primary goal of the workshop is to help the stakeholders of the medical device sector to understand what the mandatory use of EUDAMED will mean and raise awareness on the timelines for its use.

By attending, participants will gain a clear understanding of how EUDAMED works, what information to provide, and when to integrate it into their regulatory processes.

Registration

Please complete the registration form by 5 May for physical participation and 12 May for online participation in the Stuttgart workshop. Once you submit the online registration form, we will process your attendance request. You will receive a confirmation or refusal email regarding your participation within a few working days.

Please note that registration (both physical and online) for the workshops in Rome and Brussels will open at a later stage.

We recommend checking this website regularly for updates.

Organising Team
eudamed-events@cecoforma.com

Register

Registration is open until 5 May for physical participation and 12 May for online participation.
Participation is subject to approval.

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